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ACTIVE NOT RECRUITING
NCT05120830
PHASE1/PHASE2

NTLA-2002 in Adults With Hereditary Angioedema (HAE)

Sponsor: Intellia Therapeutics

View on ClinicalTrials.gov

Summary

This study will be conducted to evaluate the safety, tolerability, activity, pharmacokinetics, and pharmacodynamics of NTLA-2002 in adults with Hereditary Angioedema (HAE).

Official title: Phase 1/2 Study to Evaluate Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of NTLA-2002 in Adults With Hereditary Angioedema (HAE)

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

INTERVENTIONAL

Enrollment

37

Start Date

2021-12-10

Completion Date

2026-07

Last Updated

2026-03-24

Healthy Volunteers

No

Interventions

BIOLOGICAL

Biological NTLA-2002

CRISPR/Cas9 gene editing system delivered by LNP for IV administration

OTHER

Normal Saline IV Administration

The administration of IV normal saline

Locations (9)

Clinical Trial Site

Campbelltown, Australia

Clinical Trial Site

Grenoble, France

Clinical Trial Site

Lille, France

Clinical Trial Site

Paris, France

Clinical Trial Site

Berlin, Germany

Clinical Trial Site

Frankfurt, Germany

Clinical Trial Site

Amsterdam, Netherlands

Clinical Trial Site

Auckland, New Zealand

Clinical Trial Site

Cambridge, United Kingdom